COMPOUNDERS
Report
- Report Number
- 6000001-2012-14005
- Event Type
- Malfunction
- Date Received
- September 10, 2012
- Date of Event
- August 17, 2012
- Report Date
- August 17, 2012
- Manufacturer
- BAXTER HEALTHCARE - LARGO
- Product Code
- NEP
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- OTHER
Narratives
(B)(4). EVALUATION SUMMARY:THE REPORTED CONDITION OF "THE FLUSH KEY ON THE KEYPAD IS NOT WORKING" WAS CONFIRMED AND REPRODUCED DURING DEVICE EVALUATION. THE ROOT CAUSE WAS DUE TO A MISSING NYLON WASHER ELECTRODE. THE NYLON WASHER ELECTRODE WAS INSTALLED TO CORRECT THE REPORTED CONDITION.
(B)(4). INITIAL EVALUATION CONFIRMED THE REPORTED CONDITION. UPON COMPLETION OF BAXTER'S INVESTIGATION, A FOLLOW-UP WILL BE SUBMITTED.
(B)(4). THE DEVICE WAS RETURNED TO BAXTER AND IS CURRENTLY IN THE PROCESS OF BEING EVALUATED. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF THE EVALUATION OR IF ANY ADDITIONAL DETAILS BECOME AVAILABLE. THIS DEVICE IS CLASS II EXEMPT FROM HAVING A 510(K) NUMBER. ITS ADDITIONAL 510(K) NUMBER IS K961008.
BAXTER RECEIVED A REPORT FROM A FACILITY INVOLVING AN AUTOMIX 3+3/AS COMPOUNDER. ACCORDING TO THE FACILITY, THE FLUSH KEY ON THE KEYPAD IS NOT WORKING. THIS EVENT OCCURRED DURING SETUP IN THE PHARMACY. THE UNIT IS BEING SWAPPED. THERE WAS NO PATIENT INVOLVEMENT; THEREFORE, NO PATIENT INJURY, MEDICAL INTERVENTION, OR ADVERSE REACTION IS ASSOCIATED WITH THE REPORTED CONDITION. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | COMPOUNDERS | SYSTEM/DEVICE, PHARMACY COMPOUNDING | NEP | BAXTER HEALTHCARE - LARGO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |